chr13-101847189-T-G

Position:

• chr13-101847189-T-G

Variant summary

Our verdict is Benign. Variant got -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_004115.4(FGF14):​c.408+21536A>C variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.607 in 151,782 control chromosomes in the GnomAD database, including 28,500 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.61 (28500 hom., cov: 32)
• Consequence: FGF14 NM_004115.4 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.491

Genes affected

FGF14 (HGNC:3671): (fibroblast growth factor 14) The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. A mutation in this gene is associated with autosomal dominant cerebral ataxia. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2008]

ACMG classification

Verdict is Benign. Variant got -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BA1: GnomAd4 highest subpopulation (EAS) allele frequency at 95% confidence interval = 0.733 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
FGF14	NM_004115.4	c.408+21536A>C		intron_variant		ENST00000376143.5	NP_004106.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
FGF14	ENST00000376143.5	c.408+21536A>C		intron_variant		1	NM_004115.4	ENSP00000365313.4

Frequencies

GnomAD3 genomes AF: 0.607 AC: 92017 AN: 151664 Hom.: 28466 Cov.: 32

Gnomad AFR AF: 0.719

Gnomad AMI AF: 0.553

Gnomad AMR AF: 0.616

Gnomad ASJ AF: 0.569

Gnomad EAS AF: 0.753

Gnomad SAS AF: 0.697

Gnomad FIN AF: 0.550

Gnomad MID AF: 0.665

Gnomad NFE AF: 0.530

Gnomad OTH AF: 0.591

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.607 AC: 92099 AN: 151782 Hom.: 28500 Cov.: 32 AF XY: 0.610 AC XY: 45238 AN XY: 74130

Gnomad4 AFR AF: 0.719

Gnomad4 AMR AF: 0.616

Gnomad4 ASJ AF: 0.569

Gnomad4 EAS AF: 0.753

Gnomad4 SAS AF: 0.698

Gnomad4 FIN AF: 0.550

Gnomad4 NFE AF: 0.530

Gnomad4 OTH AF: 0.596

Alfa AF: 0.565 Hom.: 13276

Bravo AF: 0.614

Asia WGS AF: 0.734 AC: 2547 AN: 3478

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	4.7
DANN	Benign	0.60

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs2984842; hg19: chr13-102499539;